Диссертация (Новые подходы к синтезу неароматических серо- и азотсодержащих гетероциклов), страница 66
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Org. Chem. 2009. – P. 2635–2641.[225]Kozhushkov S. I., Langer R., Yufit D. S., Howard J. A. K., Schill H., Demus D., MiyazawaK., de Meijere A. Novel liquid crystalline compounds containing bicyclo[3.1.0]hexane coreunits // Eur.
J. Org. Chem. 2004. – P. 289–303.[226]Allen F. H. The geometry of small rings. I. Substituent-induced bond-length asymmetry incyclopropanes // Acta Crystallogr., Sect. B. 1980. – Vol. 36. – P. 81–96.[227]Danishefsky S. Electrophilic cyclopropanes in organic synthesis // Acc. Chem. Res. 1979. –Vol. 12. – P. 66–72.[228]Hattori K., Grossman R. B. Functionalized cis- and trans-fused bicyclic α-amino acids viastereoselective double annulation and dequaternisation reactions // J. Org. Chem. 2003.
– Vol.68. – P. 1409–1417.[229]Miranda L. S. M., Vasconcellos M. L. A. A. Chemoselective RuO4 oxidation of phenyl or pmethoxyphenyl groups to carboxylic acid functions in the presence of a tetrahydropyran ring //Synthesis. 2004. – P. 1767–1770.[230]Mewshawand R. E., Commons T. J. J.
Synthesis and antibacterial activity of C-4 substitutedmonobactams // Antibiotics. 1987. – Vol. 40. – P. 1563–1571.[231]Grunder-Klotz E., Ehrhardt J.-D. The 3,4-dimethoxybenzyl moiety as a new N-protectinggroup of 1,2-thiazetidine 1,1-dioxides // Tetrahedron Lett. 1991. – Vol. 32. – P. 751–752.[232]Rassadin V. A., Grosheva D. S., Tomashevskiy A. A., Sokolov V. V., Yufit D. S.,Kozhushkov S. I., de Meijere A.
Bicyclic sultams with a nitrogen at the bridgehead and a268sulfur atom in the apex position: facile preparation and conformational properties // Eur. J.Org. Chem. 2010. – P. 3481–3486.[233] Paquette L. A., Leit S. M. The first examples of bridgehead bicyclic sultams // J. Am. Chem.Soc. 1999. – Vol. 121. – P. 8126–8127.[234] Paquette L. A., Barton W. R. S., Gallucci J.
C. Synthesis of 1-aza-8-thiabicyclo[4.2.1]nona-2,4diene 8,8-dioxide and it’s conversion to a strained spirocycle via photoinduced SO2−N bondcleavage // Org. Lett. 2004. – Vol. 6. – P. 1313–1315.[235] Evans P., McCabe T., Morgan B. S., Reau S. Double reduction of cyclic aromaticsulfonamides: a novel method for the synthesis of 2- and 3-aryl-substituted cyclic amines //Org. Lett. 2005. – Vol. 7.
– P. 43–46.[236] Preston A. J., Gallucci J. C., Paquette L. A. Synthesis and selected reactions of a bicyclicsultam having sulfur at the apex position // J. Org. Chem. 2006. – Vol. 71. – P. 6573–6578.[237] Hall H. K., Shaw R. G., Deutschmann A. Anti-Bredt molecules. 2. 1-Azabicyclo[3.3.1]nonan2-one, a new bicyclic lactam containing bridgehead nitrogen // J. Org. Chem. 1980.
– Vol. 45.– P. 3722–3724.[238] Steliou K., Poupart M. A. Reagents for organic synthesis. Part 3. Tin-mediated esterification inmacrolide synthesis // J. Am. Chem. Soc. 1983. – Vol. 105. – P. 7130–7138.[239] Brehm R., Ohnha D., Gerlach H. Synthese und Bestimmung des Chiralitätssinns von (+)-(R)-1Azabicylo[3.3.1]nonan-2-on // Helv. Chim. Acta.
1987. – Vol. 70. – P. 1981–1987.[240] Zefirov N. S., Rogozina S. V. Stereochemical studies – XVIII: conformational study ofheteroanalogues of bicyclo[3.3.1]nonane // Tetrahedron. 1974. – Vol. 30. – P. 2345–2352.[241] Грошева Д. С. Синтез сультамов из сульфонамидов с дополнительной CH-кислотнойгруппой путём внутримолекулярной реакции Михаэля // Вып. квалиф. работа спец. С.Петербург: СПбГУ, 2014. – 120 с.[242] Wojciechowski K. Synthesis of nitrobenzophenones from nitro--sulfonyldiphenylmethanederivatives // Synth. Commun. 1997. – Vol. 27.
– P. 135–144.[243] Wojciechowski K., Kosiński S. Synthesis of novel isothiazolo[4,3-b]pyridine andisothiazolo[4,3-b]quinoline derivatives // Tetrahedron. 2001. – Vol. 57. – P. 5009–5014.[244] Yang Z., Xu J. Synthesis of benzo--sultams via the Rh-catalyzed aromatic C–Hfunctionalization of diazosulfonamides // Chem. Commun. 2014. – Vol. 50. – P. 3616–3618.[245]Togo H., Harada Y., Yokoyama M. Preparation of 3,4-dihydro-2,1-benzothiazine 2,2-dioxideskeleton from N-methyl 2-(aryl)ethanesulfonamides with (diacetoxyiodo)arenes // J. Org.Chem.
2000. – Vol. 65. – P. 926–929.269[246]Togo H., Misu Y. Novel preparation of 2,1-benzothiazine derivatives from sulfonamides with[hydroxy(tosyloxy)iodo]arenes // Org. Biomol. Chem. 2003. – Vol. 1. – P. 1342–1346.[247]Moroda A., Furuyama S., Togo H. Facile preparation of 3,4-dihydro-2,1-benzothiazine 2,2dioxides and related reaction with 1,3-diiodo-5,5-dimethylhydantoin under photochemicalconditions // Synlett. 2009.
– P. 1336–1340.[248]Yamaura M., Suzuki T., Hashimoto H., Yoshimura J., Okamoto T., Shin C. Oxidative removalof N-(4-methoxybenzyl) group on 2,5-piperazinediones with cerium(IV) diammonium nitrate// Bull. Chem. Soc. Jpn. 1985. – Vol. 58. – P. 1413–1420.[249]Davies S. G., Mujtaba N., Roberts P. M., Smith A. D., Thomson J. E. A tandem conjugateaddition/cyclization protocol for the asymmetric synthesis of 2-aryl-4-aminotetrahydroquinoline-3-carboxylic acid derivatives // Org. Lett. 2009. – Vol. 11. – P. 1959–1962.[250]Hurtley W.
R. H. Replacement of halogen in ortho-bromobenzoic acid // J. Chem. Soc. 1929.– P. 1870–1873.[251]Xie X., Cai G., Ma D. CuI/L-proline-catalyzed coupling reactions of aryl halides withactivated methylene compounds // Org. Lett. 2005. – Vol. 7. – P. 4693–4695.[252] Yip S. F., Cheung H. Y., Zhou Z., Kwong F. Y. Room-temperature copper-catalyzed αarylation of malonates // Org. Lett. 2007. – Vol.
9. – P. 3469–3472.[253] Jiang Y., Wu N., Wu H., He M. An efficient and mild CuI/l-proline-catalyzed arylation ofacetylacetone or ethyl cyanoacetate // Synlett. 2005. – P. 2731–2734.[254] Uno M., Seto K., Takahashi S. A new method of synthesis of arylmalononitriles catalysed by apalladium complex // J. Chem. Soc., Chem. Commun. 1984.– P. 932–933.[255] Uno M., Seto K., Ueda W., Masuda M., Takahashi S. A convenient synthesis of alkylarylcyanoacetates by palladium-catalyzed aromatic substitution // Synthesis.
1985. – P. 506–508.[256] Sakamoto T., Katoh E., Kondo Y., Yamanaka H. Cross-coupling of N-heteroaryl halides withactive methylene compounds in the presence of tetrakis(triphenylphosphine)palladium // Chem.Pharm. Bull. 1988. – Vol. 36. – P. 1664–1668.[257] Sakamoto T., Katoh E., Kondo Y., Yamanaka H. Palladium-catalyzed condensation of arylhalides with phenylsulfonylacetonitrile and diethyl cyanomethylphosphonate // Chem. Pharm.Bull.
1990. – Vol. 38. – P. 1513–1517.[258] Kashin A. N., Mitin A. V., Beletskaya I. P., Wife R. Palladium-catalyzed arylation of sulfonylCH-acids // Tetrahedron Lett. 2002. – Vol. 43. – P. 2539–2542.[259] Mitin A. V., Kashin A. N., Beletskaya I. P. Role of base in palladium-catalyzed arylation ofcarbanions // J. Organomet. Chem. 2004. – Vol. 689. – P. 1085–1090.270[260] Zeevaart J.
G., Parkinson C. J., de Koning C. B. Palladium-catalysed arylation of sulfonamidestabilised enolates // Tetrahedron Lett. 2005. – Vol. 46. – P. 1597–1599.[261] Grimm J. B., Katcher M. H., Witter D. J., Northrup A. B. A new strategy for the synthesis ofbenzylic sulfonamides: palladium-catalyzed arylation and sulfonamide metathesis // J. Org.Chem. 2007.
– Vol. 72. – P. 8135–8138.[262] Cacchi S., Fabrizi G., Goggiamani A. 2,3-Disubstituted indoles through the palladiumcatalyzed reaction of aryl chlorides with o-alkynyltrifluoroacetanilides // Adv. Synth. Catal.2006. – Vol. 348. – P. 1301–1305.[263] Kraus G. A., Guo H. Flexible synthesis of 2,3-disubstituted indoles from aminobenzylphosphonium salts. A direct synthesis of rutaecarpine // J. Org. Chem. 2009. – Vol. 74. – P.5337–5341.[264] Wojciechowski K. Aza-ortho-xylylenes in organic synthesis // Eur.
J. Org. Chem. 2001. – P.3587–3605.[265] Wojciechowski K. Reactions of aza-ortho-xylylenes generated from 2,1-benzisothiazoline 2,2dioxides // Tetrahedron. 1993. – Vol. 49. – P. 1217–1286.[266] Dolomanov O. V., Bourhis L. J., Gildea R. J., Howard J. A. K., Puschmann H. OLEX2: acomplete structure solution, refinement and analysis program // J.
Appl. Cryst. 2009. – Vol. 42.– P. 339–341.[267] CrysAlisPro. Agilent Technologies. Version 1.171.36.20 (release 27.06.2012).[268] Brown H. C., Zweifel G. Hydroboration. IX. The hydroboration of cyclic and bicyclic olefins –stereochemistry of the hydoboration reaction // J. Am. Chem. Soc. 1961. – Vol. 83. – P. 2544–2551.[269] Huang D.
W. W., Wang W. Synthesis of [2,3-3H]-n-butyl alcohol // J. Labelled Comp. 1997. –Vol. 39. – P. 349–352.[270] Brandsma L. Preparative acetylenic chemistry, 2nd edition. – Amsterdam: Elsevier. 1988. P.48.[271] Петров А. А. О порядке присоединения галогеноводородов к галогенпроизводнымокисей триметилэтилена и изопропилэтилена // ЖОХ. 1945. – Т. 15. – С. 931–939.[272] Schuetz R. D., Jacobs R.
L. The preparation and desulfurization of some unsymmetricallysubstituted thiiranes // J. Org. Chem. 1961. – Vol. 26. – P. 3467–3471.[273] Moore C. G., Trego B. R. The reaction of triphenylphosphine with organic disulphides andpolysulphides // Tetrahedron. 1962. – Vol. 18. – P. 205–218.[274] von Braun J. Ueber Cyan-benzolsulfamide primärer Basen // Ber. Deutsch. Chem. Ges. 1904. –Vol. 37. – P. 2809–2812.271[275] Hinsberg O. Ueber einige Benzolsulfamide und gemischte secundäre Amine // Lieb. Ann.Chem. 1891. – Vol.
